Hashiba H, Hosoi J, Karasawa M, Yamada S, Nose K, Kuroki T
Department of Cancer Cell Research, University of Tokyo, Japan.
Mol Carcinog. 1989;2(2):95-100. doi: 10.1002/mc.2940020208.
A single topical application of 12-O-tetradecanoylphorbol-13-acetate (TPA) was found to induce mRNA of a metallothionein (MT) gene or genes in the skin of Sencar mice, and papillomas produced by repeated applications of TPA were shown to have elevated levels of MT mRNA. Induction of MT mRNA was maximal 4-8 h after application of TPA and returned to the control level 24 h later. A dose-dependent increase of MT mRNA was observed with doses of TPA of 1-5 micrograms. Of the other promoters tested, phorbol-12, 13-didecanoate, mezerein, and the ionophore A23187 also induced MT mRNA, but 4-O-methyl-TPA and benzoyl peroxide did not. Phorbol and 4 alpha-phorbol-12,13-didecanoate, which are not promoters, also did not induce MT mRNA. Retinoic acid and 1 alpha, 25-dihydroxyvitamin D3, inhibitors of tumor promotion, did not induce MT mRNA themselves or inhibit the induction of MT mRNA by TPA. In C57BL/6 promotion-resistant mice, TPA caused only slight induction of MT mRNA. These data suggest a correlation between induction of MT mRNA and epidermal hyperplasia. The constitutive elevation of MT mRNA levels in papillomas may be due to the loss, during the process of tumor promotion, of some mechanism regulating MT gene expression.
研究发现,单次局部应用12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)可诱导Sencar小鼠皮肤中一种或多种金属硫蛋白(MT)基因的mRNA表达,且多次应用TPA产生的乳头状瘤显示MT mRNA水平升高。TPA应用后4 - 8小时MT mRNA的诱导达到最大值,24小时后恢复到对照水平。当TPA剂量为1 - 5微克时,观察到MT mRNA呈剂量依赖性增加。在所测试的其他促癌剂中,佛波醇 - 12,13 - 二癸酸酯、大戟二萜醇酯和离子载体A23187也能诱导MT mRNA,但4 - O - 甲基 - TPA和过氧化苯甲酰则不能。非促癌剂佛波醇和4α - 佛波醇 - 12,13 - 二癸酸酯也不能诱导MT mRNA。肿瘤促进抑制剂视黄酸和1α,25 - 二羟基维生素D3本身不能诱导MT mRNA,也不能抑制TPA对MT mRNA的诱导。在C57BL / 6抗促癌小鼠中,TPA仅引起MT mRNA的轻微诱导。这些数据表明MT mRNA的诱导与表皮增生之间存在相关性。乳头状瘤中MT mRNA水平的组成性升高可能是由于在肿瘤促进过程中,某些调节MT基因表达的机制丧失所致。